CN103987729B - 癌胚抗原相关细胞粘附分子(ceacam)的抗体 - Google Patents
癌胚抗原相关细胞粘附分子(ceacam)的抗体 Download PDFInfo
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- A61K2239/00—Indexing codes associated with cellular immunotherapy of group A61K39/46
- A61K2239/46—Indexing codes associated with cellular immunotherapy of group A61K39/46 characterised by the cancer treated
- A61K2239/57—Skin; melanoma
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- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
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Applications Claiming Priority (3)
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PCT/IL2011/000808 WO2013054320A1 (fr) | 2011-10-11 | 2011-10-11 | Anticorps dirigés contre la molécule d'adhésion cellulaire associée à l'antigène carcino-embryonnaire (ceacam) |
ILPCT/IL2011/000808 | 2011-10-11 | ||
PCT/IL2012/050402 WO2013054331A1 (fr) | 2011-10-11 | 2012-10-10 | Anticorps dirigés contre la molécule d'adhésion cellulaire associée à l'antigène carcinoembryonnaire (ceacam) |
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US (3) | US9771431B2 (fr) |
EP (2) | EP2744829B1 (fr) |
JP (1) | JP6170926B2 (fr) |
KR (1) | KR102189409B1 (fr) |
CN (1) | CN103987729B (fr) |
AU (1) | AU2012322272C1 (fr) |
BR (1) | BR112014008893B1 (fr) |
CA (1) | CA2851762C (fr) |
ES (2) | ES2661488T3 (fr) |
HK (1) | HK1199646A1 (fr) |
IL (1) | IL231931B (fr) |
IN (1) | IN2014MN00873A (fr) |
LT (1) | LT2744829T (fr) |
PL (2) | PL3360899T3 (fr) |
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Families Citing this family (111)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1909827A4 (fr) * | 2005-06-09 | 2010-03-10 | Gal Markel | Modulation de l'immunite et de l'activite de ceacam1 |
ES2563527T3 (es) * | 2009-04-30 | 2016-03-15 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Anticuerpos anti-CEACAM1 y métodos de uso de los mismos |
DK3138581T3 (en) | 2011-03-17 | 2019-04-15 | Univ Birmingham | REDIRECTED IMMUNTERY |
WO2015075710A1 (fr) * | 2013-11-25 | 2015-05-28 | Ccam Biotherapeutics Ltd. | Compositions comprenant des anticorps anti-ceacam1, agents d'activation des lymphocytes et lymphocytes activés pour une cancérothérapie |
JP6879739B2 (ja) | 2013-11-25 | 2021-06-02 | フェイムウェイヴ リミテッド | 癌治療のための抗ceacam1および抗pd抗体を含む組成物 |
EP4026909A1 (fr) | 2013-12-19 | 2022-07-13 | Novartis AG | Récepteurs antigéniques chimériques de la mésothéline humaine et leurs utilisations |
US20170044268A1 (en) * | 2013-12-23 | 2017-02-16 | OncoMed Pharmaceuticals | Immunotherapy with Binding Agents |
WO2015101996A1 (fr) * | 2014-01-02 | 2015-07-09 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Anticorps à ceacam1 et inhibiteurs de kinase destinés au traitement de cellules à mutation de braf |
JOP20200094A1 (ar) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | جزيئات جسم مضاد لـ pd-1 واستخداماتها |
JOP20200096A1 (ar) | 2014-01-31 | 2017-06-16 | Children’S Medical Center Corp | جزيئات جسم مضاد لـ tim-3 واستخداماتها |
EP3116909B1 (fr) | 2014-03-14 | 2019-11-13 | Novartis Ag | Molécules d'anticorps anti-lag-3 et leurs utilisations |
EP3593812A3 (fr) | 2014-03-15 | 2020-05-27 | Novartis AG | Traitement du cancer à l'aide d'un récepteur d'antigène chimérique |
IL307423A (en) | 2014-04-07 | 2023-12-01 | Novartis Ag | Cancer treatment using chimeric antigen receptor (CAR) against CD19 |
US11427647B2 (en) | 2014-04-27 | 2022-08-30 | Famewave Ltd. | Polynucleotides encoding humanized antibodies against CEACAM1 |
CA2946262C (fr) * | 2014-04-27 | 2022-07-26 | Ccam Biotherapeutics Ltd. | Anticorps humanises diriges contre ceacam1 |
US9753036B2 (en) * | 2014-04-29 | 2017-09-05 | Edp Biotech Corporation | Methods and compositions for screening and detecting biomarkers |
WO2016014530A1 (fr) | 2014-07-21 | 2016-01-28 | Novartis Ag | Combinaisons de faibles doses renforçant l'immunité d'inhibiteurs de mtor et car |
WO2016014553A1 (fr) | 2014-07-21 | 2016-01-28 | Novartis Ag | Récepteurs d'antigènes chimères synthétisés par l'intermédiaire d'une sortase |
SG11201700416TA (en) | 2014-07-21 | 2017-02-27 | Novartis Ag | Treatment of cancer using a cd33 chimeric antigen receptor |
ES2781175T3 (es) | 2014-07-31 | 2020-08-31 | Novartis Ag | Subconjunto optimizado de células T que contienen un receptor de antígeno quimérico |
US10851149B2 (en) | 2014-08-14 | 2020-12-01 | The Trustees Of The University Of Pennsylvania | Treatment of cancer using GFR α-4 chimeric antigen receptor |
SG11201700770PA (en) | 2014-08-19 | 2017-03-30 | Novartis Ag | Anti-cd123 chimeric antigen receptor (car) for use in cancer treatment |
EP3191126B1 (fr) | 2014-09-13 | 2020-05-13 | Novartis AG | Thérapies combinées d'inhibiteurs d'alk |
BR112017005390A2 (pt) | 2014-09-17 | 2017-12-12 | Novartis Ag | células citotóxicas alvo com receptores quiméricos para imunoterapia adotiva |
MX2017004360A (es) | 2014-10-03 | 2017-06-26 | Novartis Ag | Terapias de combinacion. |
KR20170068504A (ko) | 2014-10-08 | 2017-06-19 | 노파르티스 아게 | 키메라 항원 수용체 요법에 대한 치료 반응성을 예측하는 바이오마커 및 그의 용도 |
WO2016061142A1 (fr) | 2014-10-14 | 2016-04-21 | Novartis Ag | Molécules d'anticorps de pd-l1 et leurs utilisations |
WO2016090034A2 (fr) | 2014-12-03 | 2016-06-09 | Novartis Ag | Méthodes de pré-conditionnement de cellules b dans une thérapie car |
US20170340733A1 (en) | 2014-12-19 | 2017-11-30 | Novartis Ag | Combination therapies |
WO2016120331A1 (fr) | 2015-01-28 | 2016-08-04 | Karl Sebastian Lang | Anticorps anti-cd66 agonistes pour la thérapie antivirale |
WO2016126611A1 (fr) | 2015-02-02 | 2016-08-11 | The University Of Birmingham | Complexes d'épitope de peptide de fragment de ciblage ayant une pluralité d'épitopes de lymphocyte t |
US11161907B2 (en) | 2015-02-02 | 2021-11-02 | Novartis Ag | Car-expressing cells against multiple tumor antigens and uses thereof |
ES2876974T3 (es) | 2015-04-07 | 2021-11-15 | Novartis Ag | Combinación de terapia con receptor de antígeno quimérico y derivados de amino pirimidina |
CA2982996A1 (fr) | 2015-04-17 | 2016-10-20 | David Maxwell Barrett | Procedes pour ameliorer l'efficacite et l'expansion de cellules exprimant un recepteur antigenique chimerique |
WO2016172583A1 (fr) | 2015-04-23 | 2016-10-27 | Novartis Ag | Traitement du cancer à l'aide de protéine récepteur antigénique chimérique et un inhibiteur de protéine kinase |
AR105433A1 (es) | 2015-07-21 | 2017-10-04 | Novartis Ag | Métodos para mejorar la eficacia y expansión de las células inmunes |
US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
EP3317301B1 (fr) | 2015-07-29 | 2021-04-07 | Novartis AG | Polythérapies comprenant des molécules d'anticorps dirigées contre lag-3 |
CN108025051B (zh) | 2015-07-29 | 2021-12-24 | 诺华股份有限公司 | 包含抗pd-1抗体分子的联合疗法 |
EP3344996A2 (fr) | 2015-09-03 | 2018-07-11 | The Trustees Of The University Of Pennsylvania | Biomarqueurs prédictifs du syndrome de libération de cytokines |
EP4046655A1 (fr) | 2015-11-03 | 2022-08-24 | Janssen Biotech, Inc. | Anticorps se liant spécifiquement à pd-1 et leurs utilisations |
WO2017106656A1 (fr) | 2015-12-17 | 2017-06-22 | Novartis Ag | Molécules d'anticorps anti-pd-1 et leurs utilisations |
US11433136B2 (en) | 2015-12-18 | 2022-09-06 | The General Hospital Corporation | Polyacetal polymers, conjugates, particles and uses thereof |
EP3389711A1 (fr) | 2015-12-18 | 2018-10-24 | Novartis AG | Anticorps ciblant cd32b et leurs procédés d'utilisation associés |
CN109069597A (zh) | 2015-12-22 | 2018-12-21 | 诺华股份有限公司 | 间皮素嵌合抗原受体(car)和抗pd-l1抗体抑制剂联用于抗癌治疗 |
CA3016287A1 (fr) | 2016-03-04 | 2017-09-08 | Novartis Ag | Cellules exprimant de multiples molecules de recepteur d'antigene chimere (car) et leurs utilisations |
CN107345969A (zh) * | 2016-05-05 | 2017-11-14 | 中国医学科学院基础医学研究所 | 包含afp、gp73和ceacam1的血清标记物在诊断肝脏疾病中的用途 |
CN107345968A (zh) * | 2016-05-05 | 2017-11-14 | 中国医学科学院基础医学研究所 | Cecam1蛋白作为血清标记物在诊断肝脏疾病中的用途 |
US11365252B2 (en) | 2016-07-20 | 2022-06-21 | University Of Utah Research Foundation | CD229 CAR T cells and methods of use thereof |
WO2018019380A1 (fr) * | 2016-07-28 | 2018-02-01 | Universität Duisburg-Essen | Anticorps anti-ceacam1 immunostimulateur |
SG10201913823VA (en) | 2016-10-07 | 2020-03-30 | Novartis Ag | Chimeric antigen receptors for the treatment of cancer |
CA3045508A1 (fr) | 2016-12-03 | 2018-06-07 | Juno Therapeutics, Inc. | Procedes de modulation de lymphocytes t modifies par car |
WO2018106738A1 (fr) | 2016-12-05 | 2018-06-14 | Massachusetts Institute Of Technology | Polymères en étoile à bras en brosse, conjugués et particules, et leurs utilisations |
KR102019913B1 (ko) * | 2017-03-24 | 2019-09-09 | 재단법인 목암생명과학연구소 | 항-ceacam1 항체 및 이의 용도 |
NZ756585A (en) * | 2017-03-24 | 2022-09-30 | Green Cross Corp | Anti-ceacam1 antibody and use thereof |
KR102325944B1 (ko) * | 2017-11-30 | 2021-11-12 | 재단법인 목암생명과학연구소 | 항-ceacam1 항체 및 이의 용도 |
US20200179511A1 (en) | 2017-04-28 | 2020-06-11 | Novartis Ag | Bcma-targeting agent, and combination therapy with a gamma secretase inhibitor |
EP3615055A1 (fr) | 2017-04-28 | 2020-03-04 | Novartis AG | Cellules exprimant un récepteur antigénique chimérique ciblant le bcma, et polythérapie comprenant un inhibiteur de gamma sécrétase |
CA3065120A1 (fr) | 2017-06-02 | 2018-12-06 | Juno Therapeutics, Inc. | Articles de fabrication et procedes de traitement utilisant une therapie cellulaire adoptive |
WO2018229715A1 (fr) | 2017-06-16 | 2018-12-20 | Novartis Ag | Compositions comprenant des anticorps anti-cd32b et procédés d'utilisation correspondants |
EP3644721A1 (fr) | 2017-06-29 | 2020-05-06 | Juno Therapeutics, Inc. | Modèle murin pour évaluer des toxicités associées à des immunothérapies |
EP3700933A1 (fr) | 2017-10-25 | 2020-09-02 | Novartis AG | Anticorps ciblant cd32b et leurs procédés d'utilisation |
CN111511370A (zh) | 2017-11-01 | 2020-08-07 | 朱诺治疗学股份有限公司 | 对b细胞成熟抗原具有特异性的抗体和嵌合抗原受体 |
US12031975B2 (en) | 2017-11-01 | 2024-07-09 | Juno Therapeutics, Inc. | Methods of assessing or monitoring a response to a cell therapy |
KR20200116077A (ko) | 2017-11-01 | 2020-10-08 | 주노 쎄러퓨티크스 인코퍼레이티드 | B 세포 성숙 항원에 특이적인 키메라 항원 수용체 및 암호화 폴리뉴클레오타이드 |
EP3724225A1 (fr) | 2017-12-15 | 2020-10-21 | Juno Therapeutics, Inc. | Molécules de liaison à l'anti-cct5 et procédés d'utilisation associés |
MA54118A (fr) | 2018-01-31 | 2021-09-15 | Celgene Corp | Polythérapie utilisant une thérapie cellulaire adoptive et un inhibiteur de point de contrôle |
EP3784351A1 (fr) | 2018-04-27 | 2021-03-03 | Novartis AG | Thérapies reposant sur des cellules car-t présentant une efficacité améliorée |
US20210396739A1 (en) | 2018-05-01 | 2021-12-23 | Novartis Ag | Biomarkers for evaluating car-t cells to predict clinical outcome |
CN112105629A (zh) * | 2018-05-09 | 2020-12-18 | 古德T细胞有限公司 | 调节性t细胞表面抗原的表位以及与其特异性结合的抗体 |
JP7438988B2 (ja) | 2018-06-13 | 2024-02-27 | ノバルティス アーゲー | Bcmaキメラ抗原受容体及びその使用 |
CN110684107B (zh) * | 2018-07-06 | 2021-03-23 | 中国人民解放军第四军医大学 | 抗MG7-Ag的单克隆抗体(MGd1)及其用途 |
CN110684108B (zh) * | 2018-07-06 | 2021-06-04 | 中国人民解放军第四军医大学 | 抗MG7-Ag的单克隆抗体(CEA37)及其用途 |
WO2020069409A1 (fr) | 2018-09-28 | 2020-04-02 | Novartis Ag | Polythérapies à base de récepteur antigénique chimérique (car) cd19 et de car cd22 |
WO2020069405A1 (fr) | 2018-09-28 | 2020-04-02 | Novartis Ag | Thérapies par récepteur antigénique chimérique (car) de cd22 |
WO2020092854A2 (fr) | 2018-11-01 | 2020-05-07 | Juno Therapeutics, Inc. | Récepteurs antigéniques chimériques spécifiques du gprc5d (élément d du groupe 5 de classe c des récepteurs couplés à la protéine g) |
WO2020092848A2 (fr) | 2018-11-01 | 2020-05-07 | Juno Therapeutics, Inc. | Méthodes pour le traitement au moyen de récepteurs antigéniques chimériques spécifiques de l'antigene de maturation des lymphocytes b |
SG11202105084VA (en) | 2018-11-16 | 2021-06-29 | Juno Therapeutics Inc | Methods of dosing engineered t cells for the treatment of b cell malignancies |
PT3886875T (pt) | 2018-11-30 | 2024-06-27 | Juno Therapeutics Inc | Métodos para tratamento utilizando terapia celular adotiva |
EP3906261A4 (fr) * | 2018-12-07 | 2022-12-21 | The Brigham And Women's Hospital, Inc. | Anticorps anti-ceacam1 humanisés et mûris par affinité |
JP2022514615A (ja) * | 2018-12-20 | 2022-02-14 | アルバート アインシュタイン カレッジ オブ メディスン | ヒト免疫チェックポイントCEACAM1(CD66a)に対するアンタゴニスト抗体及びその製剤、キット並びに使用方法 |
KR102166982B1 (ko) * | 2019-01-24 | 2020-10-16 | 가톨릭대학교 산학협력단 | 간암에서 CEACAM1 및 EpCAM의 상관관계 및 이를 이용한 간암 치료효과에 대한 정보를 제공하는 방법 |
MA54863A (fr) | 2019-01-29 | 2021-12-08 | Juno Therapeutics Inc | Anticorps et récepteurs antigéniques chimériques spécifiques du récepteur orphelin-1 de type récepteur à tyrosine kinase (ror1) |
JP2022536114A (ja) * | 2019-06-04 | 2022-08-12 | 普米斯生物技術(珠海)有限公司 | 抗ceacam5モノクローナル抗体およびその調製方法およびその使用 |
WO2021024020A1 (fr) | 2019-08-06 | 2021-02-11 | Astellas Pharma Inc. | Polythérapie impliquant des anticorps dirigés contre la claudine 18.2 et inhibiteurs de point de contrôle immunitaire pour le traitement du cancer |
JP2023501387A (ja) * | 2019-11-07 | 2023-01-18 | グリーン・クロス・コーポレイション | Ceacam1の立体エピトープ、及びceacam1の立体エピトープに特異的に結合する抗ceacam1抗体又はその断片 |
MX2022006365A (es) | 2019-11-26 | 2022-06-22 | Novartis Ag | Receptores de antigeno quimerico cd19 y cd22 y usos de los mismos. |
CA3179800A1 (fr) | 2020-04-10 | 2021-10-14 | Juno Therapeutics, Inc. | Methodes et utilisations associees a une therapie cellulaire modifiee a l'aide d'un recepteur antigenique chimerique ciblant un antigene de maturation des lymphocytes b |
EP3909601A1 (fr) | 2020-05-11 | 2021-11-17 | LeukoCom GmbH | Nouvel anticorps se liant spécifiquement au ceacam 1/3/5 humain et son utilisation |
CN111675750B (zh) * | 2020-06-11 | 2022-08-30 | 中国药科大学 | 针对癌胚抗原相关黏附分子ceacam的肿瘤靶向肽及其应用 |
AU2021306613A1 (en) | 2020-07-07 | 2023-02-02 | BioNTech SE | Therapeutic RNA for HPV-positive cancer |
CN113105549B (zh) * | 2020-08-04 | 2022-04-01 | 中山大学附属第五医院 | 抗ceacam5纳米抗体 |
IL300500A (en) | 2020-08-20 | 2023-04-01 | A2 Biotherapeutics Inc | Preparations and methods for the treatment of mesothelin positive cancer |
MX2023002017A (es) | 2020-08-20 | 2023-04-28 | A2 Biotherapeutics Inc | Composiciones y métodos para tratar cánceres positivos para ceacam. |
WO2022040470A1 (fr) * | 2020-08-20 | 2022-02-24 | A2 Biotherapeutics, Inc. | Compositions et méthodes de traitement de cancers positifs à ceacam |
WO2022041745A1 (fr) * | 2020-08-28 | 2022-03-03 | 安源医药科技(上海)有限公司 | Anticorps dirigé contre la proteine s du coronavirus sars-cov-2 et son utilisation |
WO2022135667A1 (fr) | 2020-12-21 | 2022-06-30 | BioNTech SE | Arn thérapeutique pour le traitement du cancer |
TW202245808A (zh) | 2020-12-21 | 2022-12-01 | 德商拜恩迪克公司 | 用於治療癌症之治療性rna |
WO2022135666A1 (fr) | 2020-12-21 | 2022-06-30 | BioNTech SE | Programme de traitement faisant intervenir des protéines cytokines |
WO2022147509A1 (fr) * | 2021-01-04 | 2022-07-07 | City Of Hope | Prévention et traitement de la maladie du greffon contre l'hôte (gvhd) résistante aux stéroïdes ou de la maladie du greffon contre l'hôte intestinale |
TW202307210A (zh) | 2021-06-01 | 2023-02-16 | 瑞士商諾華公司 | Cd19和cd22嵌合抗原受體及其用途 |
KR20240046323A (ko) | 2021-07-13 | 2024-04-08 | 비온테크 에스이 | 암에 대한 병용 요법에 있어서 cd40 및 cd137에 대한 다중특이 결합제 |
TW202333802A (zh) | 2021-10-11 | 2023-09-01 | 德商拜恩迪克公司 | 用於肺癌之治療性rna(二) |
WO2023250400A1 (fr) | 2022-06-22 | 2023-12-28 | Juno Therapeutics, Inc. | Méthodes de traitement pour thérapie de deuxième ligne par cellules car-t ciblées par cd19 |
WO2024031091A2 (fr) | 2022-08-05 | 2024-02-08 | Juno Therapeutics, Inc. | Récepteurs antigéniques chimériques spécifiques de gprc5d et bcma |
WO2024034580A1 (fr) * | 2022-08-08 | 2024-02-15 | 株式会社先端生命科学研究所 | Procédé de détection de ceacam1 |
WO2024035662A2 (fr) | 2022-08-10 | 2024-02-15 | Merck Sharp & Dohme Llc | Protéines se liant à nkg2d, cd16 et ceacam5 |
WO2024100663A1 (fr) * | 2022-11-10 | 2024-05-16 | Famewave Ltd. | Anticorps anti-molécule d'adhésion cellulaire liée à l'antigène carcino-embryonnaire 1 (ceacam1) pour l'inhibition d'activités médiées par des pièges extracellulaires neutrophiles (net) |
WO2024129778A2 (fr) | 2022-12-13 | 2024-06-20 | Juno Therapeutics, Inc. | Récepteurs antigéniques chimériques spécifiques de baff-r et cd19 et procédés et utilisations associés |
WO2024126457A1 (fr) | 2022-12-14 | 2024-06-20 | Astellas Pharma Europe Bv | Polythérapie impliquant des agents de liaison bispécifiques se liant à cldn18.2 et cd3 et des inhibiteurs de point de contrôle immunitaire |
WO2024165403A1 (fr) | 2023-02-06 | 2024-08-15 | Philogen S.P.A. | Anticorps anti-cea |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001013937A1 (fr) * | 1999-08-26 | 2001-03-01 | Skubitz Keith M | Peptides capables de moduler la fonction des membres de la famille cd66 (ceacam) |
WO2002068601A2 (fr) * | 2001-02-28 | 2002-09-06 | Skubitz Keith M | Peptides de petite taille a capacite de modulation de la fonction des membres de la famille des cd66 (ceacam) |
Family Cites Families (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL154600B (nl) | 1971-02-10 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van specifiek bindende eiwitten en hun corresponderende bindbare stoffen. |
NL154598B (nl) | 1970-11-10 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van laagmoleculire verbindingen en van eiwitten die deze verbindingen specifiek kunnen binden, alsmede testverpakking. |
NL154599B (nl) | 1970-12-28 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van specifiek bindende eiwitten en hun corresponderende bindbare stoffen, alsmede testverpakking. |
US3901654A (en) | 1971-06-21 | 1975-08-26 | Biological Developments | Receptor assays of biologically active compounds employing biologically specific receptors |
US3853987A (en) | 1971-09-01 | 1974-12-10 | W Dreyer | Immunological reagent and radioimmuno assay |
US3867517A (en) | 1971-12-21 | 1975-02-18 | Abbott Lab | Direct radioimmunoassay for antigens and their antibodies |
NL171930C (nl) | 1972-05-11 | 1983-06-01 | Akzo Nv | Werkwijze voor het aantonen en bepalen van haptenen, alsmede testverpakkingen. |
US3850578A (en) | 1973-03-12 | 1974-11-26 | H Mcconnell | Process for assaying for biologically active molecules |
US3935074A (en) | 1973-12-17 | 1976-01-27 | Syva Company | Antibody steric hindrance immunoassay with two antibodies |
US3996345A (en) | 1974-08-12 | 1976-12-07 | Syva Company | Fluorescence quenching with immunological pairs in immunoassays |
US4034074A (en) | 1974-09-19 | 1977-07-05 | The Board Of Trustees Of Leland Stanford Junior University | Universal reagent 2-site immunoradiometric assay using labelled anti (IgG) |
US3984533A (en) | 1975-11-13 | 1976-10-05 | General Electric Company | Electrophoretic method of detecting antigen-antibody reaction |
US4036945A (en) | 1976-05-03 | 1977-07-19 | The Massachusetts General Hospital | Composition and method for determining the size and location of myocardial infarcts |
US4098876A (en) | 1976-10-26 | 1978-07-04 | Corning Glass Works | Reverse sandwich immunoassay |
US4331647A (en) | 1980-03-03 | 1982-05-25 | Goldenberg Milton David | Tumor localization and therapy with labeled antibody fragments specific to tumor-associated markers |
US4348376A (en) | 1980-03-03 | 1982-09-07 | Goldenberg Milton David | Tumor localization and therapy with labeled anti-CEA antibody |
US4879219A (en) | 1980-09-19 | 1989-11-07 | General Hospital Corporation | Immunoassay utilizing monoclonal high affinity IgM antibodies |
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
US5011771A (en) | 1984-04-12 | 1991-04-30 | The General Hospital Corporation | Multiepitopic immunometric assay |
US4666828A (en) | 1984-08-15 | 1987-05-19 | The General Hospital Corporation | Test for Huntington's disease |
GB8422238D0 (en) | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
US4801531A (en) | 1985-04-17 | 1989-01-31 | Biotechnology Research Partners, Ltd. | Apo AI/CIII genomic polymorphisms predictive of atherosclerosis |
US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
US6022958A (en) | 1986-08-13 | 2000-02-08 | Bayer Corporation | cDNAs coding for members of the carcinoembryonic antigen family |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
GB8823869D0 (en) | 1988-10-12 | 1988-11-16 | Medical Res Council | Production of antibodies |
US5272057A (en) | 1988-10-14 | 1993-12-21 | Georgetown University | Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
IL162181A (en) | 1988-12-28 | 2006-04-10 | Pdl Biopharma Inc | A method of producing humanized immunoglubulin, and polynucleotides encoding the same |
US5096815A (en) | 1989-01-06 | 1992-03-17 | Protein Engineering Corporation | Generation and selection of novel dna-binding proteins and polypeptides |
DE3920358A1 (de) | 1989-06-22 | 1991-01-17 | Behringwerke Ag | Bispezifische und oligospezifische, mono- und oligovalente antikoerperkonstrukte, ihre herstellung und verwendung |
US5192659A (en) | 1989-08-25 | 1993-03-09 | Genetype Ag | Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes |
US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
EP0546073B1 (fr) | 1990-08-29 | 1997-09-10 | GenPharm International, Inc. | production et utilisation des animaux non humains transgeniques capable de produire des anticorps heterologues |
US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
CA2405246A1 (fr) | 1990-12-03 | 1992-06-11 | Genentech, Inc. | Methode d'enrichissement de proteines variantes aux proprietes liantes a lterees |
JP4124480B2 (ja) | 1991-06-14 | 2008-07-23 | ジェネンテック・インコーポレーテッド | 免疫グロブリン変異体 |
DE69233528T2 (de) | 1991-11-25 | 2006-03-16 | Enzon, Inc. | Verfahren zur Herstellung von multivalenten antigenbindenden Proteinen |
EP0654085B1 (fr) | 1992-01-23 | 1997-04-02 | MERCK PATENT GmbH | Proteines fusionnees monomeres et dimeres a fragments d'anticorps |
US5281521A (en) | 1992-07-20 | 1994-01-25 | The Trustees Of The University Of Pennsylvania | Modified avidin-biotin technique |
JP3659261B2 (ja) | 1994-10-20 | 2005-06-15 | モルフォシス・アクチェンゲゼルシャフト | 組換体タンパク質の多機能性複合体への標的化ヘテロ結合 |
GB9421405D0 (en) | 1994-10-21 | 1994-12-07 | Dow Chemical Co | Low voc laminating formulations |
US5641870A (en) | 1995-04-20 | 1997-06-24 | Genentech, Inc. | Low pH hydrophobic interaction chromatography for antibody purification |
DE69633175T2 (de) | 1995-05-23 | 2005-08-11 | Morphosys Ag | Multimere proteine |
US5719867A (en) | 1995-06-30 | 1998-02-17 | Scientific-Atlanta, Inc. | Plural telephony channel baseband signal demodulator for a broadband communications system |
JP4843138B2 (ja) * | 1998-04-15 | 2011-12-21 | ザ・ブリガーム・アンド・ウーメンズ・ホスピタル・インコーポレーテッド | T細胞阻害性受容体組成物およびその使用 |
DE19852804C1 (de) | 1998-11-16 | 1999-12-23 | Christoph Wagener | Beeinflussung der Angiogenese durch CD66a |
DE10016877A1 (de) | 2000-04-05 | 2001-10-18 | Scintec Diagnostics Gmbh Zug | (Glyko-)Proteine mit hoher Immunreaktivität sowie ein Verfahren zu ihrer Herstellung |
SE0002835D0 (sv) | 2000-08-07 | 2000-08-07 | Karolinska Innovations Ab | Method and kit for production of monoclonal antibodies |
US20030022292A1 (en) | 2001-06-07 | 2003-01-30 | Gray-Owen Scott D. | Ligation of CEACAM1 |
US20060058257A1 (en) | 2001-08-03 | 2006-03-16 | Christoph Wagener | Influencing angiogenesis using CD66a |
US20030190600A1 (en) | 2002-04-05 | 2003-10-09 | Dana-Faber Cancer Institute | Carcinoembryonic antigen cell adhesion molecule 1 (CEACAM1) structure and uses thereof in drug identification and screening |
US20030211477A1 (en) | 2002-04-05 | 2003-11-13 | Holmes Kathryn V. | Carcinoembryonic antigen cell adhesion molecule 1 (CEACAM1) structure and uses thereof in drug identification and screening |
CU23228A1 (en) | 2002-04-29 | 2007-09-26 | Ct Ingenieria Genetica Biotech | FRAGMENTS OF SPECIFIC ANTIBODIES FOR THE HUMAN CARCINOEMBRIONARY ANTIGEN (CEA) SEQUENCES OF ITS VARIABLE REGIONS AND VECTORS FOR THE MICROBIAL EXPRESSION OF THE SAME |
US20040047858A1 (en) | 2002-09-11 | 2004-03-11 | Blumberg Richard S. | Therapeutic anti-BGP(C-CAM1) antibodies and uses thereof |
US7803372B2 (en) | 2002-10-08 | 2010-09-28 | Immunomedics, Inc. | Antibody therapy |
AU2002332087A1 (en) | 2002-10-08 | 2004-05-04 | Immunomedics, Inc. | Combination therapy with class iii anti-cea monoclonal antibodies and therapeutic agents |
WO2005006958A2 (fr) | 2003-07-12 | 2005-01-27 | Isis Pharmaceuticals, Inc. | Modulation de l'expression de ceacam1 |
WO2005050200A2 (fr) | 2003-11-13 | 2005-06-02 | Genentech, Inc. | Dosages de criblage et procedes de traitement de tumeur |
WO2006085961A2 (fr) * | 2004-06-30 | 2006-08-17 | Centocor, Inc. | Anticorps anti-mcp-1, compositions, procedes et utilisations |
EP1909827A4 (fr) | 2005-06-09 | 2010-03-10 | Gal Markel | Modulation de l'immunite et de l'activite de ceacam1 |
US20090226444A1 (en) * | 2005-12-21 | 2009-09-10 | Micromet Ag | Pharmaceutical antibody compositions with resistance to soluble cea |
RS55181B1 (sr) * | 2005-12-21 | 2017-01-31 | Amgen Res (Munich) Gmbh | Farmaceutske kompozicije sa rezistencijom na rastvorljivi cea |
EP1988901B1 (fr) | 2006-02-27 | 2020-01-29 | Gal Markel | Agents antibactériens à base de ceacam |
HUE025636T2 (en) | 2007-07-27 | 2016-04-28 | Immatics Biotechnologies Gmbh | New immunogenic epitope for immunotherapy |
WO2009141679A2 (fr) | 2007-11-05 | 2009-11-26 | Gal Markel | Diagnostic du cancer hors laboratoire à base de ceacam1 |
US8817788B2 (en) | 2008-01-17 | 2014-08-26 | Nec Corporation | Wireless communication terminal, method, program, recording medium, and wireless communication system |
ES2563527T3 (es) | 2009-04-30 | 2016-03-15 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Anticuerpos anti-CEACAM1 y métodos de uso de los mismos |
US20120122122A1 (en) | 2009-07-21 | 2012-05-17 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Method of diagnosing cancer |
AU2010288469A1 (en) * | 2009-08-31 | 2012-03-01 | Roche Glycart Ag | Affinity-matured humanized anti CEA monoclonal antibodies |
WO2011047146A2 (fr) | 2009-10-14 | 2011-04-21 | Centocor Ortho Biotech Inc. | Procédés de maturation d'affinité d'anticorps |
US8256790B2 (en) | 2010-05-26 | 2012-09-04 | William Olen Fortner | Adjustable receiver hitch system |
WO2013100653A1 (fr) | 2011-12-27 | 2013-07-04 | 주식회사 엘지화학 | Batterie secondaire au lithium et son procédé de production |
CA2887528C (fr) | 2012-10-12 | 2023-08-29 | The Brigham And Women's Hospital, Inc. | Renforcement de la reponse immunitaire |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001013937A1 (fr) * | 1999-08-26 | 2001-03-01 | Skubitz Keith M | Peptides capables de moduler la fonction des membres de la famille cd66 (ceacam) |
WO2002068601A2 (fr) * | 2001-02-28 | 2002-09-06 | Skubitz Keith M | Peptides de petite taille a capacite de modulation de la fonction des membres de la famille des cd66 (ceacam) |
Non-Patent Citations (1)
Title |
---|
癌胚抗原相关细胞粘附分1的研究进展;金呈强等;《中国癌症杂志》;20080415;第18卷(第4期);第310-314页 * |
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